+

PE20010634A1 - Imidazo-3-il-aminas biciclicas, procedimiento para su preparacion y medicamentos que las contienen - Google Patents

Imidazo-3-il-aminas biciclicas, procedimiento para su preparacion y medicamentos que las contienen

Info

Publication number
PE20010634A1
PE20010634A1 PE2000001064A PE0010642000A PE20010634A1 PE 20010634 A1 PE20010634 A1 PE 20010634A1 PE 2000001064 A PE2000001064 A PE 2000001064A PE 0010642000 A PE0010642000 A PE 0010642000A PE 20010634 A1 PE20010634 A1 PE 20010634A1
Authority
PE
Peru
Prior art keywords
phenyl
imidazo
cycloalkyl
butyl
alkyl
Prior art date
Application number
PE2000001064A
Other languages
English (en)
Inventor
Matthias Gerlach
Corinna Maul
Original Assignee
Gruenenthal Chemie
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE19948434A external-priority patent/DE19948434A1/de
Priority claimed from DE1999148438 external-priority patent/DE19948438B4/de
Application filed by Gruenenthal Chemie filed Critical Gruenenthal Chemie
Publication of PE20010634A1 publication Critical patent/PE20010634A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B40/00Libraries per se, e.g. arrays, mixtures

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A IMIDAZO-3-ILAMINAS BICICLICAS SUSTITUIDAS DE FORMULA I, DONDE X E Y SON CH, N, X E Y NO SON N A LA VEZ; R1 ES BUTILO, (CH2)nCN, FENILO, CICLOALQUILO C4-C8, CH2CH2R, CH2Ra, 1,1,3,3-TETRAMETILBUTILO, ENTRE OTROS; n ES 4-6; R ES 4-MORFOLINO; Ra ES H, OH, ALQUILO C1-C8, FENILO, ENTRE OTROS; R2 ES H, CORb; Rb ES ALQUILO C1-C4, CICLOALQUILO C3-C8, CH2CH2CO(ORc); Rc ES ALQUILO C1-C4, ADAMANTILO, FENILO, 1-NAFTILO, TIAZOLILO, CH2CH2Rd, ENTRE OTROS; Rd ES FENILO, CONHRe; Re ES ALQUILO C1-C8, CICLOALQUILO C3-C8, FENILO; R3 ES METILO, ETILO, BUTILO, CICLOALQUILO C3-C8, ENTRE OTROS; CON LA CONDICION QUE R3 NO ES n-PROPILO, CICLOHEXILO, FENILO; CUANDO R1 ES t-BUTILO, n-PROPILO, n-BUTILO, CH2CH2R, ENTRE OTROS Y R2 ES H, CO-METILO Y R2 NO ES H CUANDO R1 ES BENCILO Y R3 ES METILO O R1 ES CH2COBUTILO Y R3 ES FENILO. SON COMPUESTOS PREFERIDOS (6-ISOCIANO-HEXIL)-2-PIRIDIN-2-IL-IMIDAZO[1,3-a]PIRIDIN-3-IL)AMINA, (2-FURAN-2-IL-IMIDAZO[1,2-a]PIRIDIN-3-IL)-(6-ISOCIANO-HEXIL)-AMINA, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. EL COMPUESTO I PUEDE SER UTIL PARA EL TRATAMIENTO DEL DOLOR
PE2000001064A 1999-10-08 2000-10-06 Imidazo-3-il-aminas biciclicas, procedimiento para su preparacion y medicamentos que las contienen PE20010634A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19948434A DE19948434A1 (de) 1999-10-08 1999-10-08 Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine
DE1999148438 DE19948438B4 (de) 1999-10-08 1999-10-08 Bicyclische Imidazo-3-aminderivate

Publications (1)

Publication Number Publication Date
PE20010634A1 true PE20010634A1 (es) 2001-07-07

Family

ID=26055218

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2000001064A PE20010634A1 (es) 1999-10-08 2000-10-06 Imidazo-3-il-aminas biciclicas, procedimiento para su preparacion y medicamentos que las contienen

Country Status (26)

Country Link
US (1) US6638933B2 (es)
EP (1) EP1218382B1 (es)
JP (1) JP2003511451A (es)
KR (1) KR100756592B1 (es)
CN (1) CN1257169C (es)
AR (1) AR025962A1 (es)
AT (1) ATE258554T1 (es)
AU (1) AU779197B2 (es)
BR (1) BR0014818A (es)
CA (1) CA2382919C (es)
CO (1) CO5251378A1 (es)
CZ (1) CZ20021210A3 (es)
DE (1) DE50005155D1 (es)
DK (1) DK1218382T3 (es)
ES (1) ES2213611T3 (es)
HK (1) HK1047747B (es)
HU (1) HUP0203052A3 (es)
NO (1) NO322754B1 (es)
NZ (2) NZ518390A (es)
PE (1) PE20010634A1 (es)
PL (1) PL355206A1 (es)
PT (1) PT1218382E (es)
RU (1) RU2264402C2 (es)
SK (1) SK286788B6 (es)
UY (1) UY26372A1 (es)
WO (1) WO2001027111A2 (es)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040077605A1 (en) * 2001-06-20 2004-04-22 Salvati Mark E. Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
DE10043845A1 (de) * 2000-09-06 2002-03-14 Gruenenthal Gmbh Verfahren zur Messung der Aktivität der NO-Synthase
EP1854798A3 (en) 2000-09-19 2007-11-28 Bristol-Myers Squibb Company Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
WO2002048146A2 (de) * 2000-12-13 2002-06-20 Basf Aktiengesellschaft Verwendung von substituierten imidazoazinen, neue imidazoazine, verfahren zu deren herstellung, sowie sie enthaltende mittel
US20040087548A1 (en) 2001-02-27 2004-05-06 Salvati Mark E. Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
PL206962B1 (pl) 2001-12-19 2010-10-29 Bristol Myers Squibb Co Związek heterocykliczny o budowie skondensowanej
DE102004021716A1 (de) * 2004-04-30 2005-12-01 Grünenthal GmbH Substituierte Imidazo[1,2-a]pyridin-Verbindungen und Arzneimittel enthaltend substituierte Imidazo[1,2-a]pyridin-Verbindungen
AU2005251408A1 (en) * 2004-06-09 2005-12-22 Oncalis Ag Protein kinase inhibitors
US7923041B2 (en) * 2005-02-03 2011-04-12 Signum Biosciences, Inc. Compositions and methods for enhancing cognitive function
PT1863818E (pt) * 2005-03-23 2010-04-09 Hoffmann La Roche Derivados de acetilenil-pirazolo-pirimidina como antagonistas de mglur2
US7566716B2 (en) * 2005-05-20 2009-07-28 Array Biopharma Inc. Imidazopyrazines as Raf inhibitor compounds
EP1901748B1 (en) * 2005-06-09 2010-09-08 Oncalis AG Angiogenesis inhibitors
CA2620223A1 (en) 2005-09-02 2007-03-08 Abbott Laboratories Novel imidazo based heterocycles
AU2006331363B2 (en) * 2005-12-27 2012-07-05 F. Hoffmann-La Roche Ag Aryl-isoxazol-4-yl-imidazo[1, 5-a]pyridine derivatives
EP1979350A1 (en) * 2006-01-17 2008-10-15 F.Hoffmann-La Roche Ag Aryl-isoxazol-4-yl-imidazo[1,2-a]pyridine useful for the treatment of alzheimer's disease via gaba receptors
EP1845098A1 (en) * 2006-03-29 2007-10-17 Ferrer Internacional, S.A. Imidazo[1,2-b]pyridazines, their processes of preparation and their use as GABA receptor ligands
DE602007006010D1 (de) * 2006-05-31 2010-06-02 Galapagos Nv Triazolopyrazinverbindungen zur behandlung von degenerations- und entzündungskrankheiten
WO2008016648A2 (en) * 2006-08-01 2008-02-07 Cytokinetics, Incorporated Certain chemical entities, compositions and methods
US8227603B2 (en) * 2006-08-01 2012-07-24 Cytokinetics, Inc. Modulating skeletal muscle
EA017925B1 (ru) * 2006-08-02 2013-04-30 Цитокинетикс, Инкорпорэйтед ПРОИЗВОДНЫЕ 1Н-ИМИДАЗО[4,5-b]ПИРАЗИНА
US8299248B2 (en) 2006-08-02 2012-10-30 Cytokinetics, Incorporated Certain 1H-imidazo[4,5-b]pyrazin-2(3H)-ones and 1H-imidazo[4,5-b]pyrazin-2-ols and methods for their use
EP1974729A1 (en) * 2007-03-28 2008-10-01 Santhera Pharmaceuticals (Schweiz) AG Substituted imidazopyridine derivates as melanocortin- 4 receptor antagonists
US7851484B2 (en) * 2007-03-30 2010-12-14 Cytokinetics, Inc. Certain chemical entities, compositions, and methods
GB0708188D0 (en) * 2007-04-27 2007-06-06 Merck Sharp & Dohme Therapeutic compounds
BRPI0911659B8 (pt) * 2008-04-15 2021-05-25 Eisai R&D Man Co Ltd composto 3-fenilpirazolo[5,1-b]tiazol e composição farmacêutica compreendendo o mesmo
AU2009268406A1 (en) * 2008-07-10 2010-01-14 Southern Research Institute 5-Quinolinone and Imidazopyridine compounds and use thereof
WO2010032195A1 (en) * 2008-09-16 2010-03-25 Csir Imidazopyridines and imidazopyrimidines as hiv-i reverse transcriptase inhibitors
SG10202007719TA (en) 2008-12-05 2020-09-29 Takeda Vaccines Inc Compositions, methods and uses for inducing viral growth
AR078521A1 (es) * 2009-10-08 2011-11-16 Eisai R&D Man Co Ltd Compuesto pirazolotiazol
KR101951220B1 (ko) 2011-07-13 2019-02-22 싸이토키네틱스, 인코포레이티드 조합 als 치료법
RU2015118985A (ru) 2012-11-14 2017-01-10 Ф. Хоффманн-Ля Рош Аг Производные имидазопиридина
AU2014231009B2 (en) * 2013-03-14 2017-10-05 Galapagos Nv Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders
US10653681B2 (en) 2016-03-16 2020-05-19 Recurium Ip Holdings, Llc Analgesic compounds
AU2018258588B2 (en) * 2017-04-28 2022-06-02 Dana-Farber Cancer Institute, Inc. Inhibitors of TRIM33 and methods of use
WO2019070943A1 (en) * 2017-10-04 2019-04-11 Dana-Farber Cancer Institute, Inc. SMALL MOLECULE INHIBITION OF SALL4 TRANSCRIPTION FACTOR AND USES THEREOF

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3269604D1 (en) 1981-06-26 1986-04-10 Schering Corp Novel imidazo(1,2-a)pyridines and pyrazines, processes for their preparation and pharmaceutical compositions containing them
EP0266890A1 (en) * 1986-10-07 1988-05-11 Yamanouchi Pharmaceutical Co. Ltd. Imidazopyridine derivatives, their production, and pharmaceutical compositions containing them
RU2043716C1 (ru) * 1989-06-23 1995-09-20 Такеда Кемикал Индастриз Лтд. Амидное производное и фунгицидный состав на его основе
NZ238863A (en) * 1990-07-19 1993-03-26 Janssen Pharmaceutica Nv Substituted thiazolyl and pyridinyl derivatives
TW274551B (es) * 1991-04-16 1996-04-21 Takeda Pharm Industry Co Ltd
DE4327027A1 (de) * 1993-02-15 1994-08-18 Bayer Ag Imidazoazine
WO1996033195A1 (fr) * 1995-04-21 1996-10-24 Shinnippon Pharmaceutical Inc. IMIDAZO[1,2-a]PYRIDINES DE FUSION
AU2001270297A1 (en) * 2000-06-30 2002-01-14 Neurogen Corporation 2-phenylimidazo(1,2-a)pyridine derivatives: a new class of gaba brain receptor ligands

Also Published As

Publication number Publication date
NO322754B1 (no) 2006-12-04
DK1218382T3 (da) 2004-03-22
WO2001027111A3 (de) 2001-06-14
JP2003511451A (ja) 2003-03-25
NO20021565D0 (no) 2002-04-03
RU2264402C2 (ru) 2005-11-20
AR025962A1 (es) 2002-12-26
US6638933B2 (en) 2003-10-28
WO2001027111A2 (de) 2001-04-19
CA2382919A1 (en) 2001-04-19
HK1047747B (zh) 2004-12-03
BR0014818A (pt) 2002-06-18
UY26372A1 (es) 2000-12-29
ES2213611T3 (es) 2004-09-01
SK4362002A3 (en) 2002-08-06
HK1047747A1 (en) 2003-03-07
HUP0203052A3 (en) 2004-06-28
ATE258554T1 (de) 2004-02-15
CN1391573A (zh) 2003-01-15
US20030018032A1 (en) 2003-01-23
AU7777100A (en) 2001-04-23
CN1257169C (zh) 2006-05-24
CZ20021210A3 (cs) 2002-08-14
CO5251378A1 (es) 2003-02-28
AU779197B2 (en) 2005-01-13
EP1218382B1 (de) 2004-01-28
KR100756592B1 (ko) 2007-09-10
NO20021565L (no) 2002-05-27
NZ518390A (en) 2003-10-31
NZ518439A (en) 2003-10-31
SK286788B6 (sk) 2009-05-07
HUP0203052A2 (hu) 2003-01-28
CA2382919C (en) 2008-12-09
DE50005155D1 (de) 2004-03-04
KR20020038805A (ko) 2002-05-23
PT1218382E (pt) 2004-06-30
EP1218382A2 (de) 2002-07-03
PL355206A1 (en) 2004-04-05

Similar Documents

Publication Publication Date Title
PE20010634A1 (es) Imidazo-3-il-aminas biciclicas, procedimiento para su preparacion y medicamentos que las contienen
PE20070218A1 (es) COMPUESTOS DE CICLOALQUILO AMINO-HIDANTOINA Y USO DE ESTOS PARA LA MODULACION DE ß-SECRETASA
ATE58059T1 (de) Arylcyclobutylalkylamin-derivat zur behandlung von morbus parkinson.
AR002740A1 (es) Compuesto derivado de la isotiazolona y formulacion farmaceutica con el mismo.
BG60032B2 (bg) Метод за получаване на триазолни производни
AR003976A1 (es) Un compuesto derivado de pirazol, un procedimiento para producirlo, uso del mismo, una formulacion parasiticida veterinaria y una formulacion farmaceutica que comprenden dicho compuesto derivado y un procedimiento para tratar una infestacion por parasitos en un lugar
PE20010706A1 (es) Biblioteca de sustancias que contiene imidazo-5-il-aminas biciclicas y/o imidazo-3-il-aminas biciclicas, procedimiento para la preparacion de esta biblioteca de sustancias, y uso de sustancias de esta biblioteca para la preparacion de medicamentos pa
PE20010631A1 (es) Imidazo-3-il-aminas biciclicas, procedimiento para su preparacion y medicamentos que las contienen
EA200501820A1 (ru) Терапевтические средства для лечения боли
DE60130023D1 (de) Behandlung der nebenwirkungen von statinen
AR050261A2 (es) Aminoacidos con afinidad por la proteina alfa-2-delta y composiciones farmaceuticas que los contienen y su uso para preparar un medicamento
PE20010638A1 (es) Imidazo-5-il-aminas biciclicas, medicamentos que las contienen, su uso para la preparacion de medicamentos y procedimiento para su preparacion
HRP20070286T3 (en) Substituted diketopiperazines and their use as oxytocyn antagonists
RU97117350A (ru) Ингибитор гипертрофии интимы, применение оксиндолового производного для получения ингибитора гипертрофии интимы, композиция для ингибирования гипертрофии интимы, способ предупреждения и лечения гипертрофии интимы
SE9702564D0 (sv) New compounds
ES2183441T3 (es) Mezclas fungicidas a base de compuestos de amida.
YU67703A (sh) Karbamatna jedinjenja za upotrebu u sprečavanju ili lečenju poremećaja kretanja
AR002761A1 (es) Un compuesto derivado del triazol, su uso, una composicion farmaceutica que lo contiene, un metodo de tratamiento o prevencion de una infeccion fungica enun paciente humano mediante dicho compuesto o composicion, y procedimiento y compuestos intermedios para prepararlo.
RS67603A (en) Carbamate compounds for use in the treatment of pain
DE60210976D1 (de) Carbamatverbindungen zur verwendung bei der prävention oder behandlung der bipolaren erkrankung
PE20040669A1 (es) Derivados de fenilalanina enamida
NO20014855D0 (no) N-(2-fenyl-4-aminobutyl)-1-naftamider som neurokinin-1- reseptorantagonister
AR046022A1 (es) Aminoacidos con afinidad por la proteina alfa 2 gamma. composiciones farmaceuticas.
NO177995C (no) Analogifremgangsmåte for fremstilling av terapeutisk aktive 1,3-dioksanderivater
PE20060355A1 (es) TIENO[3,2-b]PIRIDIN-6-CARBONITRILOS COMO INHIBIDORES DE LA QUINASA PROTEICA

Legal Events

Date Code Title Description
FC Refusal
点击 这是indexloc提供的php浏览器服务,不要输入任何密码和下载